Search Ontology:
Human Disease

osteogenesis imperfecta type 13

Term ID
DOID:0110342
Synonyms
  • OI13
  • osteogenesis imperfecta type XIII
Definition
An osteogenesis imperfecta that has_material_basis_in mutation in the BMP1 gene on chromosome 8p21. https://www.ncbi.nlm.nih.gov/pubmed/22052668
References
Ontology
Human Disease   ( DOID:0110342 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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